chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140644040140644041TC45GENIChomozygous114030705
5140644151140644152AG36GENIChomozygous114030706
5140644265140644265CT33GENIChomozygous128246908
5140646029140646030GA57GENIChomozygous114030711
5140646989140646990GA62GENIChomozygous114030712
5140648010140648011TC36GENIChomozygous114030713
5140648273140648274GC36GENIChomozygous114030714
5140648865140648866GA50GENIChomozygous114030715
5140649127140649128TC44GENIChomozygous114030716
5140649674140649675CT47GENIChomozygous114030717
5140649872140649873CT43GENIChomozygous114030718
5140650229140650230CG27GENIChomozygous114030719
5140650234140650235GA26GENIChomozygous114030720
5140650944140650945TA38GENIChomozygous114030721
5140651082140651083TC46GENIChomozygous114030722
5140651255140651256AC64GENIChomozygous114030723
5140651278140651279TC68GENIChomozygous114030724
5140651285140651286TC68GENIChomozygous114030725
5140652635140652636TC41GENIChomozygous114030726
5140652873140652874CT56GENIChomozygous114030727
5140653387140653388G13GENIChomozygous128246909
5140653474140653475GA34GENIChomozygous114030728
5140653564140653565CT42GENIChomozygous114030729
5140653736140653737G30GENIChomozygous128246910
5140653740140653741TC29GENIChomozygous114030730
5140653749140653749GAGGAGGAG32GENIChomozygous128246911
5140654163140654164AG42GENIChomozygous114030731
5140654216140654217TG29GENICpossibly homozygous114030732
5140654249140654250AG26GENIChomozygous114030733
5140654307140654308AG23GENIChomozygous114030735
5140654694140654695AT19GENICpossibly homozygous114030736
5140654737140654739TT26GENIChomozygous128246912
5140655340140655341GA69GENIChomozygous114030737
5140655484140655485CA55GENIChomozygous114030738
5140650300140650405CCAGGGCTGCATAGTGAGACCCTGTCCAAATAACAAAACAAACGAGGGTTTCCCAGGAGGTGTTGGCGCATGACTCTAATCTGGGCACTTAAGAAATAGAGAGTC31GENICheterozygous129917113
5140655668140655669AG53GENIChomozygous114030739